Quality Assurance Specialist

1 day ago


Baltimore, Maryland, United States C-Care Full time
Job Title: Quality Control Technician

At C-Care, we are seeking a highly skilled Quality Control Technician to join our team. As a Quality Control Technician, you will play a critical role in ensuring the manufacturing process meets quality and efficiency standards.

Key Responsibilities:
  • Assist in the inspection and testing of received and in-process materials, components, and products to ensure adherence to established quality standards.
  • Perform quality checks, including start-up procedures, 30-minute checks, pallet check assessments, labeling assessments, product organoleptic evaluations, and batch-related information assurance.
  • Ensure that quality checks are maintained in accordance with the site Quality Management Program.
  • Assist in the development of an enhanced quality control process within C-Care, including warehouse, receiving, mixing/compounding, and filling areas.
  • Collaborate with the Quality Control Manager and Director of Quality to drive deviation reporting and non-conformity observations from all areas of the facility.
  • Assist in the development of a robust, communicative, and controlled quality process with the Director of Quality and Technical Services Manager.
  • Voice and escalate concerns, including quality deviations, employee safety, and/or management issues, and all hazard control areas within the facility.
  • Demonstrate proactive thinking and critical, rapid correction as needed.
  • Assist in the development and evaluation of new procedures and protocols with the Director of Quality.
  • Verify checklist paperwork and/or electronic records daily.
  • Deliver quality results and recordkeeping.
  • Attend EHS meetings and discuss potential risks and issues.
  • Maintain critical awareness of all areas of the facility with respect to quality and hazard control.
Requirements:
  • B.S. or B.A. in a related field.
  • 2+ years of prior experience in a quality control role with direct experience in observing product quality within a manufacturing process and environment.
  • Prior experience with reviewing batch records, start-up records, 30-minute checklists, and all other quality documentation for verification purposes is preferred.
  • Prior training as an ISO 22716 Lead Auditor and Internal Auditing, HACCP, and FDA GMP/OTC guidelines within 21 CFR is a plus.
  • Ability to work independently without supervision in a deadline-driven environment.
  • Ability to communicate effectively with all levels of management, both written and orally.
  • Must be detail-oriented with excellent organizational skills.
  • Prior experience with MS Office applications like Word and Excel.
  • Availability and willingness to work flexible hours, including some nights and weekends, to meet customer needs.


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